| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80358297 | 1.000 | 0.080 | 11 | 86951423 | missense variant | T/G | snv | 1 | |||
| rs80358301 | 1.000 | 0.080 | 11 | 86951272 | inframe deletion | CCACAT/- | delins | 1 | |||
| rs80358303 | 1.000 | 0.080 | 11 | 86951254 | frameshift variant | AG/- | delins | 1 |